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Oxidation of Chromium(III) to (VI) by Manganese Oxides

Jae Gon Kima, Joe B. Dixon*,a, Charles C. Chusueib and Youjun Denga

a Dep. of Soil and Crop Sciences, Texas A&M Univ., College Station, TX 77843-2474
b Dep. of Chemistry, P.O. Box 30012, Texas A&M Univ., College Station, TX 77842-3012



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Fig. 1. X-ray diffraction patterns of the coarse clay-size (0.2–2 µm) Mn oxides (synthetic pyrolusite and natural lithiophorite, todorokite, and birnessite). The unit of d-spaces in the figures is angstroms (Å). The XRD peaks marked with * stand for silicates.

 


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Fig. 2. Infrared curves of the coarse clay-size Mn oxides (%T equals % transmission).

 


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Fig. 3. Transmission electron micrographs of (a) todorokite (b) birnessite, (c) lithiophorite, and (d) pyrolusite.

 


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Fig. 4. Bar graphs of relative binding energy of Mn 2p3/2 for todorokite (T), birnessite (B), lithiophorite (L), and pyrolusite (P).

 


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Fig. 5. Binding energy curves O 1s electrons in the four Mn oxides. The abbreviations are todorokite (T), birnessite (B), lithiophorite (L), and pyrolusite (P).

 


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Fig. 6. Kinetics of Cr oxidation by the coarse clay-size Mn oxides at pH 4. The oxidation tests were conducted at (a) 200 µM and at (b) 400 µM of initial Cr(III) concentration. Data were plotted according to the first-order rate equation (Sparks, 1989). Concentration: Kt = Cr(III) at time t; K{infty}= Cr(III) at equilibrium.

 


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Fig. 7. Chromium oxidation by four Mn oxides in 12 h at pH 4 and 7. The four Mn oxides are abbreviated as follows: todorokite (T), birnessite (B), lithiophorite (L), and pyrolusite (P).

 





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